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rs587783595

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587783595(A;A)
Make rs587783595(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position10812271
GeneDNM2
is asnp
is mentioned by
dbSNPrs587783595
ebirs587783595
HLIrs587783595
Exacrs587783595
Varsomers587783595
Maprs587783595
PheGenIrs587783595
hapmaprs587783595
1000 genomesrs587783595
hgdprs587783595
ensemblrs587783595
gopubmedrs587783595
geneviewrs587783595
scholarrs587783595
googlers587783595
pharmgkbrs587783595
gwascentralrs587783595
openSNPrs587783595
23andMers587783595
23andMe allrs587783595
SNP Nexus

SNPshotrs587783595
SNPdbers587783595
MSV3drs587783595
GWAS Ctlgrs587783595
Max Magnitude0
ClinVar
Risk rs587783595(A;A)
Alt rs587783595(A;A)
Reference rs587783595(G;G)
Significance Pathogenic
Disease Myopathy
Variation info
Gene DNM2
CLNDBN Myopathy, centronuclear
Reversed 0
HGVS NC_000019.9:g.10922947G>A
CLNSRC
CLNACC RCV000145903.1,